×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
MGD
Deletions of exon 50 of the dystrophin gene are among the most common single exon deletions causing DMD .
29187645
2017
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
MGD
Effect of genetic background on the dystrophic phenotype in mdx mice.
26566673
2016
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
MGD
The first exon duplication mouse model of Duchenne muscular dystrophy: A tool for therapeutic development.
26365037
2015
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
RGD
Characterization of dystrophin deficient rats: a new model for Duchenne muscular dystrophy .
25310701
2014
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
RGD
Duchenne muscular dystrophy (DMD ) is an X-linked lethal muscle disorder caused by mutations in the Dmd gene encoding Dystrophin .
25005781
2014
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
MGD
mdx(⁵cv) mice manifest more severe muscle dysfunction and diaphragm force deficits than do mdx Mice.
21893021
2011
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
MGD
Duchenne muscular dystrophy (DMD ) is an X-linked recessive genetic disease caused by mutations in the gene coding for the protein dystrophin .
20705734
2010
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
MGD
Genetic background affects properties of satellite cells and mdx phenotypes.
20304955
2010
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
MGD
Osteopontin promotes fibrosis in dystrophic mouse muscle by modulating immune cell subsets and intramuscular TGF-beta.
19451692
2009
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
MGD
Muscular dystrophy begins early in embryonic development deriving from stem cell loss and disrupted skeletal muscle formation.
19535499
2009
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
MGD
Cerebellar synaptic defects and abnormal motor behavior in mice lacking alpha- and beta-dystrobrevin.
16540561
2006
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
MGD
Cardiac sodium channel Nav1.5 is regulated by a multiprotein complex composed of syntrophins and dystrophin.
16857961
2006
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
MGD
Since production of multiple dystrophin isoforms due to alternative splicing or exon skipping is totally prevented in the DMD -null mouse, these new mutants will provide an improved model system for functional studies of dystrophin and its isoforms.
15694376
2005
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
MGD
Lack of dystrophin is known to be the cause of Duchenne muscular dystrophy (DMD ).
12148865
2002
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
MGD
Muscle plasma membrane changes in dystrophin gene exon 52 knockout mouse.
11432672
2001
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
MGD
Dmd(mdx-beta geo): a new allele for the mouse dystrophin gene.
9626497
1998
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
MGD
Exon 52 of the dystrophin gene was disrupted, because the deletion of this exon is known to result in the DMD phenotype in human.
9299538
1997
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
MGD
mdxCv3 mouse is a model for electroretinography of Duchenne/Becker muscular dystrophy.
7843915
1995
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
MGD
The pituitary-muscle axis in mdx dystrophic mice.
8064326
1994
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
MGD
Sodium is elevated in mdx muscles: ionic interactions in dystrophic cells.
8433102
1993
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
MGD
The frequency of revertants in mdx mouse genetic models for Duchenne muscular dystrophy.
1635838
1992
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
MGD
Recovery of induced mutations for X chromosome-linked muscular dystrophy in mice.
2919177
1989
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
MGD
The mdx mouse skeletal muscle myopathy: I. A histological, morphometric and biochemical investigation.
2967442
1988
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
MGD
Muscle fiber growth and necrosis in dystrophic muscles: a comparative study between dy and mdx mice.
3440862
1987
×
Entrez Id:
1756
Gene Symbol:
DMD
DMD
Muscular Dystrophy, Duchenne
1.000
Biomarker
MGD
X chromosome-linked muscular dystrophy (mdx) in the mouse.
6583703
1984